KR20020006676A - 193㎚ 석판인쇄술용 하이드록시-아미노 열 경화된 하도제 - Google Patents
193㎚ 석판인쇄술용 하이드록시-아미노 열 경화된 하도제 Download PDFInfo
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- KR20020006676A KR20020006676A KR1020017011501A KR20017011501A KR20020006676A KR 20020006676 A KR20020006676 A KR 20020006676A KR 1020017011501 A KR1020017011501 A KR 1020017011501A KR 20017011501 A KR20017011501 A KR 20017011501A KR 20020006676 A KR20020006676 A KR 20020006676A
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- methacrylate
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- C09D125/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring; Coating compositions based on derivatives of such polymers
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Abstract
Description
| 실시예 | 중합체 1(g) | 가교결합제(g) | 열 산 생성제(g) | PGMEA(g) | 조밀한 선의 해상도(㎛) | 분리된 선의 해상도(㎛) |
| 5 | 2.75 | 0.15 | 0.11 | 17 | 0.14 | 0.13 |
| 6 | 2.60 | 0.30 | 0.11 | 17 | 0.14 | 0.13 |
| 7 | 2.70 | 0.23 | 0.08 | 17 | 0.14 | 0.12 |
| 8 | 2.81 | 0.15 | 0.05 | 17 | 0.14 | 0.13 |
| 9 | 2.41 | 0.27 | 0.04 | 15.4 | 0.14 | 0.12 |
| 10 | 3.71 | 0.68 | 0.11 | 25.5 | 0.15 | 0.13 |
| 11 | 3.94 | 0.45 | 0.11 | 25.5 | 0.14 | 0.12 |
| 12 | 4.16 | 0.23 | 0.11 | 25.5 | 0.15 | 0.13 |
| 실시예 | 중합체(g) | 가교결합제(g) | 열 산 생성제(g) | PGMEA(g) | 조밀한 선의 해상도(㎛) | 분리된 선의 해상도(㎛) |
| 13 | 3.84 | 0.53 | 0.13 | 25.5 | 0.15 | 0.13 |
| 14 | 3.84 | 0.53 | 0.13 | 25.5 | 0.15 | 0.13 |
Claims (33)
- 사이클로헥산올, 하이드록시스티렌, 하이드록시알킬 아크릴레이트 또는 메타크릴레이트, 하이드록시사이클로알킬 아크릴레이트 또는 메타크릴레이트, 하이드록시알킬사이클로알킬 아크릴레이트 또는 메타크릴레이트, 아릴알킬 알콜 및 알릴 알콜로 이루어진 그룹으로부터 선택된 단량체 단위를 포함하는 하이드록실 함유 중합체, 아미노 가교결합제 및 열 산 생성제를 포함하는 열 경화가능한 중합체 조성물.
- 제1항에 있어서, 하이드록실 함유 중합체가 사이클로헥산올, 하이드록시스티렌, 하이드록시알킬 아크릴레이트 또는 메타크릴레이트, 바이페닐 아크릴레이트 또는 메타크릴레이트 및 하이드록시사이클로알킬 아크릴레이트 또는 메타크릴레이트 단량체 단위를 포함하고 하이드록실 함유 중합체의 수 평균 분자량이 약 14,000 내지 30,000인 조성물.
- 제1항에 있어서, 열 산 생성제가 화학식의 화합물[여기서, R7은 치환되거나 치환되지 않은 알킬, 사이클로알킬 또는 방향족 그룹(여기서, 치환된 그룹은 할로겐, 알콕시, 방향족, 니트로 또는 아미노 그룹이다)이고, R8내지 R12는 독립적으로 수소, 직쇄 또는 측쇄 C1내지 C4알킬, 알콕시, 아미노, 알킬아미노, 아릴, 알케닐, 할로겐, 아실옥시, 사이클로알킬, 또는 고리형 사이클로알킬, 방향족 화합물 또는 헤테로사이클릭 화합물로부터 선택된다]인 조성물.
- 제1항에 있어서, 아미노 가교결합제가 화학식의 화합물[여기서, Y는 NR5R6또는 치환되거나 치환되지 않은 아릴 또는 알킬 그룹이고, R1내지 R6은 독립적으로 수소 또는 화학식 -CH2OH 또는 CH2OR17의 그룹(여기서, R17은 탄소수 약 1 내지 8의 알킬 그룹이다)이다]인 조성물.
- 제1항에 있어서, 하이드록실 함유 중합체가 알릴 알콜 단량체 단위를 포함하고 중합체 중량 평균 분자량이 2,000 내지 20,000인 조성물.
- 제1항에 있어서, 아크릴산 또는 메타크릴산의 지환족 에스테르 단량체 단위를 추가로 포함하는 조성물.
- 제6항에 있어서, 아크릴산 또는 메타크릴산의 지환족 에스테르 단량체 단위가 사이클로헥실 아크릴레이트, 사이클로헥실 메타크릴레이트, 4-3급-부틸사이클로헥실 아크릴레이트, 4-3급-부틸사이클로헥실 메타크릴레이트, 이소보닐 아크릴레이트, 이소보닐 메타크릴레이트 아다만틸 아크릴레이트 및 메타크릴레이트, 디사이클로펜테닐 아크릴레이트 및 메타크릴레이트, 2-(디사이클로펜테닐옥시)에틸 아크릴레이트 및 메타크릴레이트로 이루어진 그룹으로부터 선택되는 조성물.
- 제1항에 있어서, 하이드록시알킬 아크릴레이트 또는 메타크릴레이트가 하이드록시메틸 아크릴레이트 또는 메타크릴레이트, 2-하이드록시에틸 아크릴레이트 또는 메타크릴레이트, 3-하이드록시프로필 아크릴레이트 또는 메타크릴레이트, 4-하이드록시부틸 아크릴레이트 또는 메타크릴레이트, 5-하이드록시펜틸 아크릴레이트 또는 메타크릴레이트 및 6-하이드록시헥실 아크릴레이트 또는 메타크릴레이트로 이루어진 그룹으로부터 선택되는 조성물.
- 제1항에 있어서, 하이드록실 함유 중합체가 화학식(A)의단량체 단위 또는 화학식(B)의 단량체 단위(여기서, R15와 R16은 독립적으로 수소 또는 메틸이다)를 포함하는 조성물.
- 제9항에 있어서, 단량체 단위(A)가 약 25 내지 60mol%이고 단량체 단위(B)가 약 40 내지 75mol%인 조성물.
- 제1항에 있어서, 하이드록실 함유 중합체가 화학식(C)의 단량체 단위 또는 화학식(D)의 단량체 단위를 포함하는 조성물.
- 제11항에 있어서, 단량체 단위(C)가 약 39 내지 60mol%이고 단량체 단위(D)가 약 40 내지 61mol%인 조성물.
- 제3항에 있어서, 열 산 생성제가 사이클로헥실 p-톨루엔설포네이트, 멘틸 p-톨루엔설포네이트, 보닐 p-톨루엔설포네이트, 사이클로헥실 트리이소프로필벤젠설포네이트 및 사이클로헥실 4-메톡시벤젠설포네이트로 이루어진 그룹으로부터 선택되는 조성물.
- 기판(a),하이드록실 함유 중합체, 아미노 가교결합제 및 열 산 생성제로 이루어진 열 경화된 조성물을 포함하는, 기판 위의 열 경화된 하도제(b) 및열 경화된 하도제 위의 방사선 감광성 내식막 표면피막을 포함하는 사진석판 감광성 피복 기판.
- 제14항에 있어서, 하이드록실 함유 중합체가 사이클로헥산올, 하이드록시스티렌, 하이드록시알킬 아크릴레이트 또는 메타크릴레이트, 하이드록시사이클로알킬 아크릴레이트 또는 메타크릴레이트, 아릴알킬 알콜 및 알릴 알콜 단량체 단위로 이루어진 그룹으로부터 선택된 단량체 단위를 포함하는 피복 기판.
- 제14항에 있어서, 열 산 생성제가 화학식의 화합물[여기서, R7은 치환되거나 치환되지 않은 알킬, 사이클로알킬 또는 방향족 그룹(여기서, 치환된 그룹은 할로겐, 알콕시, 방향족, 니트로 또는 아미노 그룹이다)이고, R8내지 R12는 독립적으로 수소, 직쇄 또는 측쇄 C1내지 C4알킬, 알콕시, 아미노, 알킬아미노, 아릴, 알케닐, 할로겐, 아실옥시, 사이클로알킬, 또는 고리형 사이클로알킬, 방향족 화합물 또는 헤테로사이클릭 화합물로부터 선택된다]인 피복 기판.
- 제15항에 있어서, 하이드록실 함유 중합체가 하이드록시알킬 아크릴레이트 또는 메타크릴레이트 및 알릴 알콜 단위로 이루어진 그룹으로부터 선택된 단량체 단위를 포함하는 피복 기판.
- 제14항에 있어서, 하이드록실 함유 중합체가 아크릴산 또는 메타크릴산 단위의 지환족 에스테르 단량체 단위를 추가로 포함하는 피복 기판.
- 제14항에 있어서, 하이드록실 함유 중합체가 화학식(A)의단량체 단위 또는 화학식(B)의 단량체 단위(여기서, R15와 R16은 독립적으로 수소 또는 메틸이다)를 포함하는 피복 기판.
- 제19항에 있어서, 단량체 단위(A)가 약 25 내지 60mol%이고 단량체 단위(B)가 약 40 내지 75mol%인 피복 기판.
- 제14항에 있어서, 하이드록실 함유 중합체가 화학식(C)의 단량체 단위 또는 화학식(D)의 단량체 단위를 포함하는 피복 기판.
- 제21항에 있어서, 단량체 단위(C)가 약 39 내지 60mol%이고 단량체 단위(D)가 약 40 내지 61mol%인 피복 기판.
- 제14항에 있어서, 하이드록실 함유 중합체가 바이페닐 아크릴레이트 또는 메타크릴레이트 및 하이드록시에틸 아크릴레이트 또는 메타크릴레이트를 포함하는 피복 기판.
- 제23항에 있어서, 바이페닐 아크릴레이트 또는 메타크릴레이트의 양이 약 50 내지 90mol%이고 하이드록시에틸 아크릴레이트 또는 메타크릴레이트의 양이 약 10 내지 50mol%인 피복 기판.
- 제14항에 있어서, 방사선 감광성 내식막 표면피막이 규소를 함유하는 화학 증폭 내식막인 피복 기판.
- 제23항에 있어서, 방사선 감광성 표면피막이 화학식의 단량체 단위(여기서, R13은 메틸 또는 하이드록시에틸이고, R14는 수소, 메틸 또는 CH2CO2CH3이며, R15와 R16은 각각 독립적으로 수소 또는 메틸이다)로 이루어진 중합체를 포함하는 피복 기판.
- 제14항에 있어서, 아미노 가교결합제가 화학식의 화합물[여기서, Y는 NR5R6또는 치환되거나 치환되지 않은 아릴 또는 알킬 그룹이고, R1내지 R6은 독립적으로 수소 또는 화학식 -CH2OH 또는 CH2OR17의 그룹(여기서, R17은 탄소수 약 1 내지 8의 알킬 그룹이다)이다]인 피복 기판.
- 기판; 하이드록실 함유 중합체, 아미노 가교결합제 및 열 산 생성제로 이루어진 열 경화된 조성물을 포함하는, 기판 위에 배치된 열 경화된 하도제; 및 열 경화된 하도제 위에 배치된 방사선 감광성 내식막 표면피막을 포함하는 피복 기판을 형성하는 단계(a),방사선 감광성 내식막 표면피막을 화학 방사선에 화상 방식으로 노광시키는 단계(b) 및방사선 감광성 내식막 표면피막을 현상액으로 현상하여 내식막 화상을 형성하는 단계(c)를 포함하는, 릴리프 구조물의 제조방법.
- 제26항에 있어서, 하이드록실 함유 중합체가 하이드록시스티렌 단량체 단위약 30 내지 60mol%와 이소보닐 아크릴레이트 또는 메타크릴레이트 단량체 단위 40 내지 70mol%를 포함하는 방법.
- 제26항에 있어서, 하이드록실 함유 중합체가 스티렌 단량체 단위 약 39 내지 60mol%와 알릴 알콜 단량체 단위 약 40 내지 61mol%를 포함하는 방법.
- 제26항에 있어서, 바이페닐 아크릴레이트 또는 메타크릴레이트의 양이 약 50 내지 90mol%이고 하이드록시에틸 아크릴레이트 또는 메타크릴레이트의 양이 약 10 내지 50mol%인 방법.
- 제26항에 있어서, 방사선 감광성 내식막 표면피막이 화학식의 단량체 단위(여기서, R3은 메틸 또는 하이드록시에틸이고, R4는 수소, 메틸 또는 CH2CO2CH3이며, R5와 R6은 각각 독립적으로 수소 또는 메틸이다)로 이루어진 중합체를 포함하는 방법.
- 제26항에 있어서, 열 경화된 하도제 조성물을 제거하여 이의 화상을 형성하는 단계를 추가로 포함하는 방법.
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| US09/268,430 US6323287B1 (en) | 1999-03-12 | 1999-03-12 | Hydroxy-amino thermally cured undercoat for 193 NM lithography |
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-
1999
- 1999-03-12 US US09/268,430 patent/US6323287B1/en not_active Expired - Fee Related
-
2000
- 2000-03-10 EP EP05024391A patent/EP1634916B1/en not_active Expired - Lifetime
- 2000-03-10 DE DE60035030T patent/DE60035030T2/de not_active Expired - Fee Related
- 2000-03-10 DE DE60041463T patent/DE60041463D1/de not_active Expired - Fee Related
- 2000-03-10 AT AT05024391T patent/ATE421551T1/de not_active IP Right Cessation
- 2000-03-10 JP JP2000604269A patent/JP3778485B2/ja not_active Expired - Fee Related
- 2000-03-10 KR KR1020017011501A patent/KR100706565B1/ko not_active Expired - Fee Related
- 2000-03-10 WO PCT/US2000/006314 patent/WO2000054105A1/en not_active Ceased
- 2000-03-10 EP EP00916239A patent/EP1163550B1/en not_active Expired - Lifetime
- 2000-03-10 EP EP05024392A patent/EP1634917A1/en not_active Withdrawn
- 2000-03-10 AT AT00916239T patent/ATE363513T1/de not_active IP Right Cessation
- 2000-05-15 TW TW089104411A patent/TWI294990B/zh not_active IP Right Cessation
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2001
- 2001-07-09 US US09/901,933 patent/US6783916B2/en not_active Expired - Fee Related
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- 2003-12-17 JP JP2003419662A patent/JP2004199073A/ja active Pending
- 2003-12-17 JP JP2003419661A patent/JP4308639B2/ja not_active Expired - Fee Related
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Also Published As
| Publication number | Publication date |
|---|---|
| US20020007018A1 (en) | 2002-01-17 |
| WO2000054105A1 (en) | 2000-09-14 |
| US20040219454A1 (en) | 2004-11-04 |
| EP1634917A1 (en) | 2006-03-15 |
| ATE421551T1 (de) | 2009-02-15 |
| US7217497B2 (en) | 2007-05-15 |
| JP4308639B2 (ja) | 2009-08-05 |
| EP1163550B1 (en) | 2007-05-30 |
| DE60041463D1 (de) | 2009-03-12 |
| DE60035030D1 (de) | 2007-07-12 |
| JP2002539473A (ja) | 2002-11-19 |
| EP1163550A4 (en) | 2004-05-26 |
| TWI294990B (en) | 2008-03-21 |
| EP1634916B1 (en) | 2009-01-21 |
| DE60035030T2 (de) | 2008-02-07 |
| JP2004185017A (ja) | 2004-07-02 |
| EP1634916A1 (en) | 2006-03-15 |
| KR100706565B1 (ko) | 2007-04-13 |
| ATE363513T1 (de) | 2007-06-15 |
| US6323287B1 (en) | 2001-11-27 |
| US6783916B2 (en) | 2004-08-31 |
| EP1163550A1 (en) | 2001-12-19 |
| JP3778485B2 (ja) | 2006-05-24 |
| JP2004199073A (ja) | 2004-07-15 |
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